Regulatory and Start Up Specialist

Precision for Medicine(30 days ago)

RemoteFull TimeJunior$54,246 - $72,990 (estimated)Regulatory Affairs

About this role

The Regulatory and Start Up Specialist at Precision for Medicine supports the initiation and regulatory readiness of clinical trial sites within an integrated CRO environment focused on oncology and rare diseases. The role provides local regulatory expertise, ensures compliance with international and national regulations, and partners with cross-functional teams to facilitate timely study approvals and site activation. The specialist contributes to maintaining study documentation and regulatory intelligence to support overall trial quality and inspection readiness.

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Required Skills

Regulatory Submissions
CA Interaction
Project Tracking
Start-Up
IMP Release
Site Coordination
Document Management
Consent Customization
Translation Coordination
Stakeholder Communication

+5 more

Qualifications

Bachelor's Degree in Life Sciences
Registered Nurse (RN)
Pharmacy Qualification
Advanced Degree in Medical or Life Sciences (MD, PhD, PharmD)
RAC Certification
Masters in Regulatory Science

About Precision for Medicine

precisiongroupcompanies.com

The site is currently a placeholder that immediately redirects to /lander and contains no public content describing the company. Presuming it's a web-focused startup, it likely offers a SaaS platform to help businesses build high-converting landing pages and marketing funnels. Typical offerings would include a drag-and-drop page builder, A/B testing, analytics, and integrations with CRMs and email platforms to drive lead generation. Customers would be small-to-medium businesses and marketing teams seeking easy onboarding, template libraries, and conversion optimization tools.